Mobile Elements and Plant Genome Evolution, Comparative Analyses and Computational Tools

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Review
16 September 2020

Cotton is a major fiber plant, which provides raw materials for clothing, protecting humans from the harsh environment of cold or hot weathers, enriching the culture and custom of human societies. Due to its importance, the diploid and tetraploid genomes of different cotton plants have been repeatedly sequenced to obtain their complete and fine genome sequences. These valuable genome data sets revealed the evolutionary past of the cotton plants, which were recursively affected by polyploidization, with a decaploidization contributing to the formation of the genus Gossypium, and a neo-tetraploidization contributing to the formation of nowadays widely cultivated cotton plants. Post-polyploidization genome instability resulted in numerous structural changes of the genomes, such as gene loss, DNA inversion and translocation, illegitimate recombination, and accumulation of repetitive sequences, and functional innovation accompanied by elevated evolutionary rates of genes. Many these changes have been asymmetric between subgnomes of the tetraploid cottons, rendering their divergent profiles of biological regulation and function. The availability of whole-genome sequences has now paved the way to identify and clone functional genes, e.g., those relating to fiber development, and to enhance breeding efforts to cultivate cottons to produce high-yield and high-quality fibers, and to resist environmental and biological stress.

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Mini Review
26 May 2020
Additional ORFs in Plant LTR-Retrotransposons
Carlos M. Vicient
 and 
Josep M. Casacuberta
Schematic representation of LTR-retrotransposons. (A) Model Ty1/copia element. (B) Model Ty3/gypsy element. (C) Arabidopis thaliana Athila (Wright and Voytas, 2002). (D) Barley Bagy2 (Vicient et al., 2001). (E) Maize Grande (Gómez-Orte et al., 2013). (F) Rice RIRE2 (Ohtsubo et al., 1999), Wallabi and Gran3 (Wicker et al., 2007). (G) Silene latifolia Retand (Kejnovsky et al., 2006). (H) Phaseolus vulgaris PvRetro13 (Gao et al., 2014). (I) Botrytis cinerea Boty (Zhao et al., 2011).

LTR-retrotransposons share a common genomic organization in which the 5′ long terminal repeat (LTR) is followed by the gag and pol genes and terminates with the 3′ LTR. Although GAG-POL-encoded proteins are considered sufficient to accomplish the LTR-retrotransposon transposition, a number of elements carrying additional open reading frames (aORF) have been described. In some cases, the presence of an aORF can be explained by a phenomenon similar to retrovirus gene transduction, but in these cases the aORFs are present in only one or a few copies. On the contrary, many elements contain aORFs, or derivatives, in all or most of their copies. These aORFs are more frequently located between pol and 3′ LTR, and they could be in sense or antisense orientation with respect to gag-pol. Sense aORFs include those encoding for ENV-like proteins, so called because they have some structural and functional similarities with retroviral ENV proteins. Antisense aORFs between pol and 3′ LTR are also relatively frequent and, for example, are present in some characterized LTR-retrotransposon families like maize Grande, rice RIRE2, or Silene Retand, although their possible roles have been not yet determined. Here, we discuss the current knowledge about these sense and antisense aORFs in plant LTR-retrotransposons, suggesting their possible origins, evolutionary relevance, and function.

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Frontiers in Plant Science

Mass Spectrometry And New Computer-Based Tools In Plant Science Research
Edited by Letizia Bernardo, Candida Vannini, George V Popescu, Carlos E. Rodríguez-López
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16 May 2025
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